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PMID: 18955454 Published · ppublish English Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Phase III, double-blind, randomized study comparing lapatinib plus paclitaxel with placebo plus paclitaxel as first-line treatment for metastatic breast cancer.

Di Leo A, Gomez HL, Aziz Z, Zvirbule Z, Bines J, Arbushites MC, Guerrera SF, Koehler M, Oliva C, Stein SH, Williams LS, Dering J, Finn RS, Press MF

Abstract

Lapatinib, a dual tyrosine kinase inhibitor of epidermal growth factor receptor (EGFR/ErbB1) and human epidermal growth factor receptor 2 (HER-2/ErbB2), is effective against HER-2-positive locally advanced or metastatic breast cancer (MBC). This phase III trial evaluated the efficacy of lapatinib in HER-2-negative and HER-2-uncharacterized MBC. Women with MBC were randomly assigned to first-line therapy with paclitaxel 175 mg/m(2) every 3 weeks plus lapatinib 1,500 mg/d or placebo. A preplanned retrospective evaluation of HER-2 status was performed using fluorescence in situ hybridization and immunohistochemistry. The primary end point was time to progression (TTP); secondary end points were objective response rate (ORR), clinical benefit rate (CBR), event-free survival (EFS), and overall survival (OS). In the intent-to-treat population (n = 579), there were no significant differences in TTP, EFS, or OS between treatment arms, although differences in ORR and CBR were noted. In 86 HER-2-positive patients (15%), treatment with paclitaxel-lapatinib resulted in statistically significant improvements in TTP, EFS, ORR, and CBR compared with paclitaxel-placebo. No differences between treatment groups were observed for any end point in HER-2-negative patients. The most common adverse events were alopecia, rash, and diarrhea. The incidence of diarrhea and rash was significantly higher in the paclitaxel-lapatinib arm. The rate of cardiac events was low, and no difference was observed between treatment arms. Patients with HER-2-negative or HER-2-untested MBC did not benefit from the addition of lapatinib to paclitaxel. However, first-line therapy with paclitaxel-lapatinib significantly improved clinical outcomes in HER-2-positive patients. Prospective evaluation of the efficacy and safety of this combination is ongoing in early and metastatic HER-2-positive breast cancer patients.

MeSH Terms
Adult Aged Aged, 80 and over Antineoplastic Combined Chemotherapy Protocols/therapeutic use Breast Neoplasms/drug therapy,pathology Double-Blind Method Female Humans Lapatinib Middle Aged Neoplasm Metastasis Paclitaxel/administration & dosage Placebos Quinazolines/administration & dosage Receptor, ErbB-2/biosynthesis Retrospective Studies
Chemicals
Placebos Quinazolines Lapatinib Receptor, ErbB-2 Paclitaxel
Authors & Affiliations
14 authors, click to expand affiliations / ORCID
Di Leo Angelo
Sandro Pitigliani Medical Oncology Unit, Hospital of Prato, Istituto Toscano Tumori, Prato, Italy 59100. [email protected]
Gomez Henry L
Aziz Zeba
Zvirbule Zanete
Bines Jose
Arbushites Michael C
Guerrera Stephanie F
Koehler Maria
Oliva Cristina
Stein Steven H
Williams Lisa S
Dering Judy
Finn Richard S
Press Michael F
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Article Info
Journal
Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Abbr.
J Clin Oncol
ISSN
1527-7755
Published
2008-12-01
Epub
2008-00-27
Pages
5544-52
Language
English
Region
United States
NLM ID
8309333
PMCID
PMC2651098
Subset
IM
Corrections
ErratumIn
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CommentIn
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